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Experiences

Current Experience

  • Regional Country Study Manager

    Belgium
    Since April 2018

    managing Clinical trials at a regional level. Clinical operations. managing CRA's. 

    Managing clinical trials at a regional level. Clinical Operations. Managing CRA's. 

Past Experience

  • Clinical Research Associate (CRA) Belgium

    August 2015 --- August 2016

    mainly working on immune oncology Phase II and Phase III Clinical trials

    experience in start up phase, initiation, monitoring, close out visits. 

  • Clinical Research Associate (CRA) Belgium

    July 2011 --- August 2015

    mainly working on oncology Phase II and Phase III Clinical trials

    experience in start up phase, initiation, monitoring, close out visits. 

  • Clinical Research Coordinator Belgium

    May 2010 --- April 2011

    coordinating the Vaccines supply intended for the Clinical trials.

  • clinical project assistant Belgium

    April 2007 --- May 2010

    ivrs project assistant. 

  • Research Assistant Belgium

    September 2004 --- June 2005

    overseeing students' practical classes (use of softwares and work in

    Laboratory).

Personality

Self Assessment :
Result OrientedAdaptabilityAnalytical thinkingAssertivenessAttention to detailAuthenticityCollaborationCommunicativeCoordinationCuriosityEfficiencyFlexibilityIndependenceInterest in knowledgeOrganizationProactivityProblem solvingResiliencyResponsibilitySelf-confidenceSelf-disciplineService orientedSociabilityTrustWillingness to compromiseOptimism

Knowledge

Self Assessment :
NegotiationCancer ResearchCAPAClinical monitoringClinical operationsClinical researchClinical trial audits and inspectionsClinical trial managementClinical Trial Management System (CTMS)Clinical trialsCommunication SkillsComplianceContract negotiationCRFCROCTMSCustomer ServiceData cleaningData entryData ManagementDrug Supply Management activitieseCRFEDCEfficacy trialsElectronic Data Capture (EDC) EnglishEthics submission and approval processGood Clinical Practice (GCP)Healthcare industryInformed Consent DocumentsInformed Consent ProcessIVRSLife SciencesMicrosoft OfficeOncology Clinical Researchpeople managementProblem SolvingTime Management

Skills and Expertise

Self Assessment :
Analytical skills Analyze data Build and manage the Trial Master File (TMF) Interpret data Monitor a clinical study Use content management systemsAssist study siteAssist with site trainingAttend seminars, courses and meetings within and outside the companyCoach clinical staffCollaborate with principal investigatorCollaborate with project teamCommunicate with investigatorCommunicate effectively on different company levelsInformed consent processInitiate clinical trials Interact with CROsInteract with ethics committeeInteract with KOLInteract with nursesInteract with pharmacistsInteract with physicians

Education

  • Master in Bioengineering from UCL in 2004

Training and Certification

  • Clinical Project Manager in 2016 Training
  • Senior Clinical Research Associate in 2016 Training
  • Languages

    BrightOwl Assessment:
    Self Assessment:
    French
    Native
    Dutch
    Full Proficiency
    English
    Full Proficiency
    Spanish
    Elementary Proficiency
    Italian
    Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Project Manager (CPM) Project Manager
  • Locations I am interested in:
    Belgium
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    BrightOwl freelancer :    40 Hours per week
  • International:
    Yes
  • Availability:
    Jan 2019 : 100%
    Feb 2019 : 100%
    Mar 2019 : 100%
    Oct 2018 : 100%
    Nov 2018 : 100%
    Dec 2018 : 100%

Area / Region

Brussels, Belgium

Others

Driving License
  • Yes

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